Canonical Allele Identifier: PA916012755
Gene: IDS HGNC NCBI

Linked Data

ClinVar Variation Id: 92618

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_006114.1:p.Arg88Cys
CA220494
NM_006123.5:c.262C>T